Language
English
Publication Date
1-1-2023
Journal
Neuropsychopharmacology
DOI
10.1038/s41386-022-01368-4
PMID
35768568
PMCID
PMC9700860
PubMedCentral® Posted Date
6-29-2022
PubMedCentral® Full Text Version
Post-print
Abstract
Major depressive disorder is a prevalent and heterogeneous disorder with treatment resistance in at least 50% of individuals. Most of the initial studies focused on the monoamine system; however, recently other mechanisms have come under investigation. Specific to the current issue, studies show synaptic involvement in depression. Other articles in this issue report on reductions in synaptic density, dendritic spines, boutons and glia associated with stress and depression. Importantly, it appears that some drugs (e.g., ketamine) may lead to rapid synaptic restoration or synaptogenesis. Direct evidence for this comes from preclinical work. However, neuroimaging studies, such as magnetic resonance imaging (MRI) and positron emission tomography (PET), have become useful in assessing these changes in vivo. Here, we describe the use of neuroimaging techniques in the evaluation of synaptic alterations associated with depression in humans, as well as measurement of synaptic restoration after administration of ketamine. Although more research is desired, use of these techniques widen our understanding of depression and move us further along the path to targeted and effective treatment for depression.
Keywords
Humans, Depressive Disorder, Major, Ketamine, Depression, Neuroimaging, Positron-Emission Tomography, Neuroscience, Medical research
Published Open-Access
yes
Recommended Citation
Sophie E Holmes, Chadi Abdallah, and Irina Esterlis, "Imaging Synaptic Density in Depression" (2023). Faculty, Staff and Students Publications. 6014.
https://digitalcommons.library.tmc.edu/baylor_docs/6014
Included in
Medical Specialties Commons, Mental and Social Health Commons, Neurosciences Commons, Psychiatry and Psychology Commons